KJ Mini Implant System
K-Number: K151970 · 2016-10-21
ApplicantKj Meditech Co., Ltd.
Decision Date2016-10-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
KJ Mini Implant System is a medical device manufactured by Kj Meditech Co., Ltd.. It received FDA 510(k) clearance on 2016-10-21 under approval number K151970. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the KJ Mini Implant System?
KJ Mini Implant System is a medical device that received FDA 510(k) clearance on 2016-10-21. It is manufactured by Kj Meditech Co., Ltd.. The 510(k) number is K151970.
When was KJ Mini Implant System approved by the FDA?
KJ Mini Implant System received FDA 510(k) clearance on 2016-10-21, under approval number K151970.
What company makes KJ Mini Implant System?
KJ Mini Implant System is manufactured by Kj Meditech Co., Ltd..
What is the FDA product code for KJ Mini Implant System?
The FDA product code for KJ Mini Implant System is DZE.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.